Florvaag E, Elsayed S, Hammer A S
Int Arch Allergy Appl Immunol. 1986;80(1):26-32.
Horizontal isoelectric focusing (IEF) and two-dimensional sodium dodecyl sulfate polyacrylamide gel electrophoresis (2-D SDS-PAGE) combined with electrophoretic transfer (ET) and immunoautoradiography (IAR) were used to characterize the crude alder (Alnus incana) pollen extract (AI crude) and fraction AI 34. IEF resolved AI crude and AI 34 into 34 and 39 distinct protein bands, respectively, when stained with Coomassie brilliant blue. The band patterns were similar and the majority of bands were located in the pH region 4.0-7.0. After ET and IAR, the distribution of antigenic reactivities was similar to that of the protein stain. Allergenic reactivity was detected in the pH region 4.6-5.2 only, where two bands at pH 4.9 demonstrated dominating IgE-binding properties. The 2-D reference maps of AI crude and AI 34 consisted of 40 and 45 protein spots, respectively. The autoradiogram of AI crude demonstrated 35 spots capable of binding rabbit IgG. The main IgE-binding zone was located at pH 4.6-5.2 and 20 kilodaltons with an area of weaker autoradiographic signals at pH 4.6-5.2 and 40 kilodaltons. ET from polyacrylamide gels to nitrocellulose (NC) membranes was quantitative and IAR gave significant radiostaining of spots containing 0.01 and 0.1 microgram of AI crude in the IgG and IgE systems, respectively. For the characterization of the alder pollen extract, horizontal 2-D SDS-PAGE combined with ET and IAR provided a powerful supplement to conventional crossed immuno- and radioimmunoelectrophoretic techniques (CIE/CRIE).
采用水平等电聚焦(IEF)和二维十二烷基硫酸钠聚丙烯酰胺凝胶电泳(2-D SDS-PAGE)结合电泳转移(ET)和免疫放射自显影(IAR)技术,对桤木(Alnus incana)粗花粉提取物(AI粗提物)和AI 34组分进行表征。用考马斯亮蓝染色时,IEF将AI粗提物和AI 34分别分离为34条和39条不同的蛋白带。条带模式相似,大多数条带位于pH 4.0 - 7.0区域。经ET和IAR后,抗原反应性分布与蛋白质染色相似。仅在pH 4.6 - 5.2区域检测到变应原反应性,其中pH 4.9处的两条带表现出主要的IgE结合特性。AI粗提物和AI 34的二维参考图谱分别由40个和45个蛋白斑点组成。AI粗提物的放射自显影片显示有35个斑点能够结合兔IgG。主要的IgE结合区位于pH 4.6 - 5.2和20千道尔顿处,在pH 4.6 - 5.2和40千道尔顿处有较弱的放射自显影信号区域。从聚丙烯酰胺凝胶到硝酸纤维素(NC)膜的ET是定量的,IAR分别在IgG和IgE系统中对含有0.01微克和0.1微克AI粗提物的斑点进行了显著的放射染色。对于桤木花粉提取物的表征,水平2-D SDS-PAGE结合ET和IAR为传统的交叉免疫电泳和放射免疫电泳技术(CIE/CRIE)提供了有力补充。